Structure of PDB 5j64 Chain A Binding Site BS01

Receptor Information
>5j64 Chain A (length=208) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
EVETFAFQAEIAQLMSLIINTFYSNKEIFLRELISNSSDALDKIRYESLT
DPSKLDSGKELHINLIPNKQDRTLTIVDTGIGMTKADLINNLGTIAKSGT
KAFMEALQAGADISMIGQFGVGFYSAYLVAEKVTVITKHNDDEQYAWESS
AGGSFTVRTDTGEPMGRGTKVILHLKEDQTEYLEERRIKEIVKKHSQFIG
YPITLFVE
Ligand information
Ligand ID6G7
InChIInChI=1S/C14H10FN3O3/c15-10-3-1-2-4-11(10)18-13(16-17-14(18)21)9-6-5-8(19)7-12(9)20/h1-7,19-20H,(H,17,21)
InChIKeyCMOWBCZHKWQARR-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 12.01c3(cc(O)c(C=1N(C(=O)NN=1)c2c(F)cccc2)cc3)O
OpenEye OEToolkits 2.0.4c1ccc(c(c1)N2C(=NNC2=O)c3ccc(cc3O)O)F
CACTVS 3.385Oc1ccc(c(O)c1)C2=NNC(=O)N2c3ccccc3F
FormulaC14 H10 F N3 O3
Name5-(2,4-dihydroxyphenyl)-4-(2-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
ChEMBLCHEMBL3895370
DrugBank
ZINC
PDB chain5j64 Chain A Residue 301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB5j64 Protein conformational flexibility modulates kinetics and thermodynamics of drug binding.
Resolution1.38 Å
Binding residue
(original residue number in PDB)
N51 A55 K58 D93 I96 G97 M98 L107 G108 T184
Binding residue
(residue number reindexed from 1)
N36 A40 K43 D78 I81 G82 M83 L92 G93 T169
Annotation score1
Binding affinityMOAD: Kd=0.000000064M
PDBbind-CN: -logKd/Ki=6.85,Kd=140nM
Enzymatic activity
Enzyme Commision number 3.6.4.10: non-chaperonin molecular chaperone ATPase.
Gene Ontology
Molecular Function
GO:0005524 ATP binding
GO:0016887 ATP hydrolysis activity
GO:0051082 unfolded protein binding
GO:0140662 ATP-dependent protein folding chaperone
Biological Process
GO:0006457 protein folding

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:5j64, PDBe:5j64, PDBj:5j64
PDBsum5j64
PubMed29273709
UniProtP07900|HS90A_HUMAN Heat shock protein HSP 90-alpha (Gene Name=HSP90AA1)

[Back to BioLiP]